library prep kit (New England Biolabs)

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New England Biolabs library prep kit
Library Prep Kit, supplied by New England Biolabs, used in various techniques. Bioz Stars score: 97/100, based on 258 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/nebnext+ultra+ii+fs+library/NEBNext+Ultra+II+FS+DNA+PCR-free+Library+Prep+Kit+for+Illumina/pm42804711-65-13-16
Average 97 stars, based on 258 article reviews

library prep kit - by Bioz Stars, 2026-10

97/100 stars

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Article Title: Stage-specific GATA3 induction promotes ILC2 development after lineage commitment.
Article Snippet: .. Briefly, cDNA and hashtag libraries were generated using a KAPA Hifi ReadyMix (Roche, Cat#KK2601) and a NEBNext Ultra II FS library prep kit for Illumina (New England Biolabs, Cat#E7805) and then quantified using a KAPA Library Quantification Kit (Roche, Cat#KK4824). .. Sequencing was performed by Illumina Novaseq 6000 sequencer to a depth of approximately 100,000 reads per cell.

Article Title: Stage-specific GATA3 induction promotes ILC2 development after lineage commitment
Article Snippet: .. Briefly, cDNA and hashtag libraries were generated using a KAPA Hifi ReadyMix (Roche, Cat#KK2601) and a NEBNext Ultra II FS library prep kit for Illumina (New England Biolabs, Cat#E7805) and then quantified using a KAPA Library Quantification Kit (Roche, Cat#KK4824). .. Sequencing was performed by Illumina Novaseq 6000 sequencer to a depth of approximately 100,000 reads per cell.

Library Quantification:

Sequencing:

Article Title: Whole genome sequencing from dried blood spots for newborn screening of Menkes disease and 36 other actionable inherited neurometabolic disorders.
Article Snippet: Tandem mass spectrometry is currently used by the Ohio Department of Health to screen newborn infants for 36 medically actionable inborn errors of metabolism.. As a complementary test for infants with abnormal biochemical screens, whole genome sequencing (WGS) theoretically could reduce false-positive results, facilitate timely case resolution and, in some instances, indicate a more specific diagnosis than obtained initially.. Menkes disease is a X-linked recessive disorder of human copper metabolism with a predicted minimum birth prevalence of 1 in 34,810 live male births.

Article Title: NR4a1/2 deletion promotes accumulation of TCF1 + stem-like precursors of exhausted CD8 + T cells in the tumor microenvironment.
Article Snippet: .. Sequencing libraries were prepared by using NEBNext Ultra II FS library prep kit for Illumina (New England Biolabs). .. The sequencing analysis were performed by ImmunoGeneTeqs, Inc (Chiba, Japan) by a Novaseq 6000 sequencer (Illumina, San Diego, CA, USA) and a Novaseq S4 200 cycles v1.0 kit (Illumina).

Whole Complete genome sequencing:

Polymerase Chain Reaction:

Article Title: Zygosity-based sex determination in a butterfly drives hypervariability of Masculinizer .
Article Snippet: .. The genomes of 31 adult males were short- read sequenced to a median mapped coverage of 8× using a NEBNext Ultra II FS library prep kit for Illumina (New England Biolabs), with 3 PCR cycles to minimize duplicates. .. One additional male (BaM_17127D) was sequenced to higher mapped coverage (65×) using the Nextera XT PCR- free protocol.

Article Title: Zygosity-based sex determination in a butterfly drives hypervariability of Masculinizer .
Article Snippet: .. The father and six sons from the 2BF1 family were whole genome sequenced to a median mapped coverage of 10× using a NEBNext Ultra II FS library prep kit for Illumina (with 3 PCR cycles to minimize duplicates). ..

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